IP Library › Granted Patent US 11,202,775
Granted Patent B2
US 11,202,775 · App. 12/238,362 · Granted Dec 21, 2021

Methods for treatment of cancer

Inventor: Cynthia C. Bamdad (Waltham, MA)
Assignee: MINERVA BIOTECHNOLOGIES CORPORATION
A61K31/437B82Y30/00
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Quick Facts
Patent No.
US 11,202,775
App. No.
12/238,362
Granted
Dec 21, 2021
Kind
B2
Abstract

A method for treating or preventing cancer in a subject comprising administering a treatment effective amount of a chemotype 4 compound.

Claims (39)

1. A method for treating cancer in which cancerous cells express MUC1* in a subject comprising assaying for presence of MUC1* in the cancer cells, and administering a treatment effective amount of a compound comprised of the formula below to the subject in which cancer cells express MUC1*:

or a steroisomer, tautomer, pharmaceutically acceptable salt, or ester thereof, wherein,

R3 is carbocycloalkyl;

R4 is selected from alkyl, branched alkyl, cycloalkyl, and H; and

R5 is halogen, lower alkyl, haloalkyl, alkylether, —NH 2 , mono-substituted amine, di-substituted amine, cyclic amine, or H.

2. The method according to claim 1 , wherein R5 is selected from halogen, lower alkyl, haloalkyl, alkylether, and H.

3. The method according to claim 1 , wherein R5 is H, F, Cl, OCH 3 , CH 3 , CN, NO 2 , or NH 2 .

4. The method according to claim 1 , wherein R5 is selected from H, F, and Cl.

5. The method according to claim 1 , wherein R5 is H.

6. A method for treating cancer in which cancerous cells express MUC1* in a subject comprising assaying for presence of MUC1* in the cancer cells, and administering a treatment effective amount of a compound comprised of the formula below to the subject in which cancer cells express MUC1*:

or a steroisomer, tautomer, pharmaceutically acceptable salt, or ester thereof, wherein,

R3 is carbocycloalkyl;

R4 is selected from alkyl, branched alkyl, cycloalkyl, and H;

R5 is halogen, lower alkyl, haloalkyl, alkylether, —NH 2 , mono-substituted amine, di-substituted amine, cyclic amine, or H;

R6 is H or alkyl;

R7 is H or alkyl; and

R8 is H or alkyl.

7. The method according to claim 6 , wherein R5 is selected from halogen, lower alkyl, haloalkyl, alkylether, and H.

8. The method according to claim 6 , wherein R5 is H, F, Cl, OCH 3 , CH 3 , CN, NO 2 , or NH 2 .

9. The method according to claim 6 , wherein

R5 is H, F, or Cl;

R6 is H or CH 3 ;

R7 is H or CH 3 ; and

R8 is H or CH 3 .

10. The method according to claim 6 , wherein

R5 is H;

R6 is H;

R7 is H; and

R8 is H.

11. The method according to claim 1 , wherein R5 is is morpholine, pyrrolidine, piperazine or piperidine.

12. The method according to claim 1 , wherein R5 is —OCH 3 .

13. The method according to claim 2 , wherein R5 is F, Cl, Br or I.

14. The method according to claim 2 , wherein R5 is CF3.

15. The method according to claim 2 , wherein R5 is methyl, ethyl or propyl.

16. The method according to claim 6 , wherein R5 is morpholine, pyrrolidine, piperazine or piperidine.

17. The method according to claim 6 , wherein R5 is —OCH 3 .

18. The method according to claim 7 , wherein R5 is CF3.

19. The method according to claim 7 , wherein R5 is methyl, ethyl or propyl.

20. The method according to claim 7 , wherein R5 is —OCH 3 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2008
From: BAMDAD, CYNTHIA
To: MINERVA BIOTECHNOLOGIES CORPORATION
Reel/Frame 021588/0640 →
Continuity (2)
Provisional Application 60975156 · Sep 25, 2007
Related Publication 20090069367A1 · Mar 12, 2009
Cited By (2)
US 12,415,868 US 12,491,259